Spironolactone Eyedrop Favors Restoration of Corneal Integrity after Wound Healing in the Rat

Author:

Rodrigues-Braz Daniela1ORCID,Zhu Linxin1,Gélizé Emmanuelle1,Clarin Jean-Pierre2,Chatagnon Xavier2,Benzine Youcef3,Rampignon Philippe3,Thouvenin Agathe45ORCID,Bourges Jean-Louis16,Behar-Cohen Francine167ORCID,Zhao Min1ORCID

Affiliation:

1. Centre de Recherche des Cordeliers, Inserm, Université Paris Cité, Sorbonne Université, 75006 Paris, France

2. Excelvision, Fareva, 07100 Annonay, France

3. Valdepharm, Fareva, 27100 Val-de-Reuil, France

4. CNRS, Inserm, UTCBS, Université Paris Cité, 75006 Paris, France

5. Département Recherche et Développement Pharmaceutique, Agence Générale des Equipements et Produits de Santé (AGEPS), AP-HP, 75005 Paris, France

6. Ophtalmopole, AP-HP, Cochin Hospital, 75014 Paris, France

7. Hôpital Foch, Service D’ophtalmologie, 92150 Suresnes, France

Abstract

Abnormal corneal wound healing can compromise corneal transparency and lead to visual impairment. Mineralocorticoid receptor antagonists (MRA) are promising candidates to promote corneal remodeling with anti-inflammatory properties and lack gluococorticoids-associated side effects. In this preclinical study, a new polymer-free hydroxypropyl-gamma-cyclodextrin-based eyedrop containing 0.1% spironolactone (SPL), a potent but non-water-soluble MRA, was investigated for its ocular surface tolerance and efficacy in a rat model of corneal wound healing. SPL eyedrops were stable for up to 9 months at 4 °C. The formulation was well-tolerated since no morphological changes or inflammatory reactions were observed in the rat cornea after multiple daily instillations over 7 days. SPL eyedrops accelerated rat corneal wound healing, reduced corneal edema and inflammation, enhanced epithelial integrity, and improved nerve regeneration, suggesting restoration of corneal homeostasis, while potassium canrenoate, an active and soluble metabolite of SPL, had no effect. SPL eyedrops could benefit patients with impaired corneal wound healing, including that secondary to glucocorticoid therapy. Repurposing known drugs with known excipients will expedite translation to the clinic.

Funder

INSERM, INSERM Transfert, Agence National de la Recherche

EU Framework Horizon Europe Program

Publisher

MDPI AG

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Reference41 articles.

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